Use of Metal Complexes as Emitter in an Organic Light-Emitting Component and such a Component

ABSTRACT

A HEMT device including a GaN channel structure including a very thin (Al, In, Ga)N subchannel layer ( 14 ) that is disposed between a first GaN channel layer ( 12 ) and a second GaN channel layer ( 16 ), to effect band bending induced from the piezoelectric and spontaneous charges associated with the (Al, In, Ga)N subchannel layer. This GaN channel/(Al, In, Ga)N subchannel arrangement effectively disperses the 2DEG throughout the channel of the device, thereby rendering the device more linear in character (relative to a corresponding device lacking the subchannel (Al5In3Ga)N sub-layer), without substantial loss of electron mobility.

FIELD OF THE INVENTION

The present invention relates to a high electron mobility transistor (HEMT) device.

DESCRIPTION OF THE RELATED ART

Gallium nitride (GaN) and GaN-based materials have physical and electronic properties that make them attractive for high temperature, high power and high frequency microelectronic devices. These properties include wide bandgap character, low thermal carrier generation rates, high breakdown field, high electron mobility and high electron velocity.

These properties of GaN and GaN-based materials render them advantageous for use in high electron mobility transistor devices, characterized by high electron mobilities, superior charge confinement and high breakdown voltage. Room temperature radio frequency (2-10 GHz) output power>2 W/mm is enabled by such GaN and GaN-based materials.

Conventional HEMTs have a narrow peak in the distribution of electrons as a function of depth, which results in a sharp peak in transconductance and poor linearity characteristics. Attempts to improve the linearity of the device have included fabrication of HEMTs with AlGaN channels, to spread the electron distribution. Unfortunately, such devices suffer from significantly reduced electron mobility, since the two-dimensional electron gas (2DEG) is predominately contained within the AlGaN alloy and alloy scattering of the electrons is a significant effect.

It would therefore be a significant advance in the art to provide a HEMT device structure that enables control of electron distribution to produce improved device linearity, without substantial adverse affect on electron mobility characteristics of the device.

SUMMARY OF THE INVENTION

The invention relates in one aspect to a HEMT device including a GaN channel structure with a very thin (<75 Angstroms) (Al, In, Ga)N subchannel layer, e.g., an AlN or AlGaN layer, that is disposed between a main GaN channel and a second GaN channel, to effect band bending induced from the piezoelectric and spontaneous charges associated with the (Al, In, Ga)N subchannel layer, to disperse 2DEG throughout the channel of the device and achieve superior linearity and electron mobility characteristics.

As used herein, “(Al, In, Ga)N subchannel layer” in reference to the intermediate layer between the main GaN channel layer and the second GaN layer in the HEMT device of the invention refers to a layer formed of a nitride composition other than GaN per se, including one or more of aluminum, indium and gallium, wherein the metal(s) in such nitride composition are in appropriate stoichiometric relationship (i.e., Al_(x)In_(y)Ga_(z)N wherein x+y+z=1, and each of x, y and z may range in value from 0 to 1, with the proviso that z≠1). The expression “(Al, In, Ga)N” therefore includes AlN, AlInN, AlInGaN, AlGaN, InGaN and InN as alternative species. AlN and AlGaN are particularly preferred (Al, In, Ga)N species in the broad practice of the invention. It will be appreciated that the channel and subchannel layers in the practice of the invention preferably form one channel, and that the respective layers may be referred to herein as channel structures.

In one aspect, the invention relates to a HEMT device, comprising:

a lower GaN channel layer;

an intermediate (Al, In, Ga)N subchannel layer; and

an upper GaN channel layer,

wherein the intermediate (Al, In, Ga)N subchannel layer has a thickness not exceeding 75 Angstroms.

Another aspect of the invention relates to a HEMT device with a channel structure including a (Al, In, Ga)N subchannel layer disposed between a first GaN channel layer and a second GaN channel layer.

A further aspect of the invention relates to a DHFET device, comprising:

a lower GaN channel layer;

an intermediate (Al, In, Ga)N subchannel layer; and

an upper GaN channel layer,

wherein the intermediate (Al, In, Ga)N subchannel layer has a thickness not exceeding 75 Angstroms.

Yet another aspect of the invention relates to a method of improving linearity without substantial loss of electron mobility in a HEMT device, including fabricating the HEMT device with a channel structure including first and second GaN channel layers and a (Al, In, Ga)N subchannel layer therebetween.

Other aspects, features and embodiments of the invention will be more fully apparent from the ensuing disclosure and appended claims.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a schematic representation of an HEMT device structure according to one embodiment of the present invention.

FIG. 2 is a band diagram of the device of FIG. 1.

FIG. 3 is a graph of conduction band edge, E_(c), in electron volts (eV) and carrier concentration, in cm⁻³, as a function of depth in Angstroms, for a structure including a 3 nm thick GaN channel and a 0.2 nm AlN undoped subchannel.

FIG. 4 is a graph of conduction band edge, E_(c), in electron volts (eV) and carrier concentration, in cm⁻³, as a function of depth in Angstroms, for a structure including a 3 nm thick GaN channel and a 0.3 nm AlN undoped subchannel.

FIG. 5 is a graph of conduction band edge, E_(c), in electron volts (eV) and carrier concentration, in cm⁻³, as a function of depth in Angstroms, for a structure including a 4 nm thick GaN channel and a 0.2 nm AlN undoped subchannel.

FIG. 6 is a graph of conduction band edge, E_(c), in electron volts (eV) and carrier concentration, in cm⁻³, as a function of depth in Angstroms, for a structure including a 4 nm thick GaN channel and a 0.3 nm AlN undoped subchannel.

FIG. 7 is a graph of conduction band edge, E_(c), in electron volts (eV) and carrier concentration, in cm⁻³, as a function of depth in Angstroms, for a structure including a 4 nm thick GaN channel and a 0.3 nm AlN layer doped with silicon at a doping density of 10¹³ atoms/cm².

FIG. 8 is a graph of conduction band edge, E_(c), in electron volts (eV) and carrier concentration, in cm⁻³, as a function of depth in Angstroms, for a device structure including a 5 nm thick AlGaN channel, containing 5% aluminum in the AlGaN channel material.

FIG. 9 is a graph of conduction band edge, E_(c), in electron volts (eV) and carrier concentration, in cm⁻³, as a function of depth in Angstroms, for a device structure including a 2 nm GaN channel, a 0.3 nm undoped AlN layer, a 3 nm GaN channel and a 0.3 nm undoped AlN layer.

FIG. 10 is a schematic representation of a HEMT device structure including an AlN barrier layer and characterized by a sheet mobility of ˜330 Ω/square.

FIG. 11 is a schematic representation of a HEMT device structure including an AlGaN channel and an AlN barrier layer and characterized by a sheet mobility of ˜610 Ω/square.

FIG. 12 is a schematic representation of a HEMT device structure including an AlN subchannel and an AlN barrier layer and characterized by a sheet mobility of ˜460 Ω/square.

DETAILED DESCRIPTION OF THE INVENTION AND PREFERRED EMBODIMENTS THEREOF

The present invention relates to a HEMT device including a GaN channel structure with a very thin (Al, In, Ga)N subchannel layer that is disposed between a main GaN channel and a second GaN channel, e.g., below a main GaN channel and above a second GaN channel, to effect band bending induced from the piezoelectric and spontaneous charges associated with the AlInGaN subchannel layer. This GaN channel and (Al, In, Ga)N subchannel arrangement effectively disperses the 2DEG throughout the channel of the device, thereby rendering the device more linear in character (relative to a corresponding device lacking the (Al, In, Ga)N subchannel layer) without substantial loss of electron mobility characteristic of the GaN-based device.

To achieve such band bending, dispersal of 2DEG throughout the channel, high electron mobility and improved linearity, the (Al, In, Ga)N subchannel layer is desirably as thin as possible, preferably being of monolayer or near-monolayer thickness, and in any event not exceeding 75 Angstroms in thickness, and more preferably not exceeding 60 Angstroms in thickness.

It will be appreciated that in specific embodiments of the invention, the thickness of the (Al, In, Ga)N subchannel layer can vary depending on the particular (Al, In, Ga)N subchannel material being employed. In one embodiment, in which the (Al, In, Ga)N subchannel layer is constituted by AlN, such AlN subchannel layer preferably does not exceed 20 Angstroms in thickness, and may for example be 6 Angstroms or less in thickness. In another embodiment in which the (Al, In, Ga)N subchannel layer is formed of AlGaN or AlInGaN, the subchannel thickness preferably does not exceed 50 Angstroms. The choice of a specific material and thickness for the (Al, In, Ga)N subchannel layer in a given device application of the invention, can readily be made by those of ordinary skill in the art, based on the disclosure herein, without undue experimentation.

By the utilization of the (Al, In, Ga)N subchannel layer structure as an intermediate layer in a GaN channel structure formed of overlying and underlying GaN channel layers, the inventive device achieves the beneficial effects realized by AlGaN channels in GaN-based devices, but without the detrimental effect of the high degree of alloy electron scattering that is typical of such AlGaN channel GaN devices.

In one specific embodiment, the subchannel layer in the HEMT device of the invention is formed of AlN or AlGaN, which can be doped or undoped in character, e.g., doped with indium. In other embodiments, the subchannel layer is formed of AlInN or AlInGaN, with the stoichiometric composition of such material preferably being selected to provide a subchannel layer that is substantially lattice matched (within 5% of the lattice coefficient value) to the GaN channel layers adjacent to the respective surfaces of the subchannel layer.

In a particularly preferred embodiment, AlN is used as the material of the subchannel layer. In HEMT structures utilizing AlN subchannel layers in accordance with the invention, the thickness of the AlN subchannel layer can be any suitable thickness effecting the aforementioned band bending, e.g., typically being in a range of from 1 Angstrom to 30 Angstroms in thickness, more preferably in a range of from 2 Angstroms to 10 Angstroms, and most preferably in a range of from 2 Angstroms to 8 Angstroms. As a specific example, subchannel thicknesses on the order of 4 Angstroms have been advantageously employed.

In HEMT device structures utilizing AlGaN subchannel layers in accordance with the invention, the thickness of the AlGaN subchannel layer is generally greater than the thickness of a corresponding subchannel layer formed of AlN, e.g., thicker by the inverse of the aluminum fraction. Accordingly, in specific embodiments, AlGaN subchannel layers can be employed at thickness in a range of from 2 to 60 Angstroms, with a thickness range of from 4 Angstroms to 20 Angstroms being more preferred, and thickness in a range of from 4 Angstroms to 16 Angstroms being most preferred. The stoichiometric composition of the AlGaN subchannel material can be widely varied within the formula Al_(x)Ga_(1-x)N, wherein 0<x<1. In one preferred embodiment, for example, the AlGaN subchannel layer has the stoichiometric formula Al_(0.5)Ga_(0.5)N.

Other specific variations of (Al, In, Ga)N subchannel layer compositions can be employed, at various specific thicknesses, within the broad practice of the present invention. For example, the subchannel can be formed of AlInN, with the stoichiometric composition appropriately selected for lattice matching to GaN, e.g., a stoichiometric composition of Al_(0.83)In_(0.17)N.

The thickness of the subchannel layer in the GaN channel HEMT device of the invention is of fundamental importance, in providing appropriate band bending and linearity and electron distribution characteristics. If the subchannel layer is excessively thin, not enough band bending will be achieved to simultaneously provide superior linearity and superior electron distribution in the channel. Further, if the subchannel layer is excessively thick, it becomes disproportionately susceptible to the presence of morphological artifacts that render it non-continuous in character. Additionally, all or substantially all of the electrons in the channel remain in the bottom channel layer.

The thickness of the subchannel controls the effective band offset of the respective GaN channel layers, determining the distribution of electrons between the respective upper and lower GaN channels.

Typically, for good linearity and electron mobility characteristics, it is desirable to have more electrons in the top (overlying) GaN channel layer, in relation to the lower (underlying) GaN channel layer. The electron distribution between the two GaN channel layers can be efficiently controlled by choice of appropriate thickness of the (Al, In, Ga)N subchannel layer and thickness of the upper GaN channel. In preferred practice, the top channel layer should contain at least slightly more electrons than the lower channel layer, with effective distributions ranging from such slight excess of electrons in the top channel layer to an order of magnitude more electrons than in the lower GaN channel layer.

As indicated, the (Al, In, Ga)N subchannel layer may be doped or undoped in character. Suitable dopant species for such purpose include, without limitation, silicon (Si) and germanium (Ge). In general, it is desirable to avoid use of oxygen as a dopant species, since it may form DX centers in the subchannel that will deleteriously affect the device performance.

Doping may be selectively applied to modify the electronic profile of the channel, and to minimize ionized impurity scattering.

Doping densities may be of any suitable character, as readily determinable within the skill of the art without undue experimentation, based on the present disclosure. Typical doping densities for Si and Ge can be in a range of from 10¹² atoms/cm² to 2×10¹³ atoms/cm².

The thicknesses of the upper GaN layer and the bottom GaN layer (above and below the subchannel layer respectively) may be of any suitable thickness appropriate to the specific HEMT device structure. For example, when AlN subchannel layers are utilized, the upper GaN channel layer typically will be greater than 10 Angstroms in thickness, and the bottom GaN layer typically will be greater than 100 Angstroms in thickness. As another example, when AlGaN nucleation layers are utilized, the thickness of the lower GaN layer may be as low as 30 Angstroms in thickness. Thicknesses of the respective GaN layers of the channel structure in specific applications of the invention will be readily determinable within the skill of the art, based on the disclosure herein. By way of further illustrative example, in one specific embodiment, the lower GaN channel layer has a thickness of 1-2 μm, the intermediate AlN subchannel layer has a thickness of 0.2-0.4 nm, and the upper GaN channel layer has a thickness of 3-5 nm.

The channel/subchannel structure of the invention provides significant flexibility and degrees of freedom in relation to channel structures of the prior art. The thicknesses of the GaN channel layers in relation to the subchannel layer thickness can be varied significantly to achieve specific desired physical conformations and performance characteristics. For example, to achieve similar charge in the bottom GaN channel, the upper GaN channel layer may be made thicker and an AlN subchannel layer may be made thinner, while achieving a same or similar overall conformation and performance. Alternatively, n-type doping levels can be reduced in the device structure, to achieve the same result.

The channel structure of the present invention may be deployed in any suitable HEMT device design, e.g., a strain balanced HEMT providing confinement for the bottom channel layer. In one embodiment, the HEMT device is an AlN barrier HEMT.

The gallium nitride channel layers may be formed using any appropriate process or technique. For example, such layers may be formed by vapor phase techniques in which reactant gas species (e.g., ammonia, trimethylgallium) enter a growth reactor in which the substrate is disposed. The reactant gas species can be passed over the substrate to deposit an epitaxial film (e.g., of GaN incorporating nitrogen from ammonia and gallium from trimethylgallium). The process may be carried out at appropriate temperature (e.g., a temperature in a range of from 500° C. to 1200° C., or in a narrower specific temperature range of from 700° C. to 1100° C., or in an even narrower range of from 900° C. to 1000° C. The pressure in the reactor may be maintained at an appropriate level (e.g., in a range of from 20 to 950 millibar). The (Al, In, Ga)N subchannel layer may be formed using any suitable technique or a process known in the art for formation of monolayer or near-monolayer films, such as MBE, MOCVD, ALE or the like, and appropriate reagents such as those mentioned above, trimethylaluminum, trimethylindium, etc. The substrate can be a wafer of gallium nitride, silicon carbide, aluminum nitride, aluminum gallium nitride, sapphire, diamond, silicon, etc.

In a specific embodiment, the channel layer structure of the invention is employed in a double heterojunction field effect transistor (DHFET), e.g., a DHFET device in which the subchannel layer is formed of AlGaN.

Referring now to the drawings, FIG. 1 is a schematic representation of a HEMT device structure according to one embodiment of the present invention.

The HEMT device structure shown in FIG. 1 includes a substrate 10, which may be of any suitable type, e.g. a homoepitaxial GaN substrate, or alternatively a heteroepitaxial substrate formed of silicon carbide, aluminum nitride, diamond, sapphire, silicon, or other appropriate material. Although not shown, the substrate 10 may include a nucleation layer, e.g., of AlN or other suitable material, at a thickness that can for example be on the order of 2000 Angstroms. Further, strain compensation layers can be employed as necessary or desired for heteroepitaxial substrates. Such nucleation layers and strain compensation layers are well known in the art and require no detailed description here, and may advantageously form part of substrate or buffer layers in device structures of the present invention.

Overlying the substrate 10 including optional nucleation and/or strain compensation layer(s), is a GaN buffer layer 12, on which (Al, In, Ga)N subchannel layer 14 has been formed. By such arrangement, the GaN buffer layer 12 defines a lower channel region in the vicinity of (Al, In, Ga)N subchannel layer 14. Overlying the (Al, In, Ga)N subchannel layer 14 is an upper GaN channel layer 16 that defines an upper channel region in the vicinity of the subchannel layer 14. The subchannel layer in this illustrative embodiment can be formed of AlN, for example, or alternatively it can be formed of AlGaN or other suitable (Al, In, Ga)N subchannel layer material.

Overlying the upper GaN channel layer 16 is an optional AlN barrier 18. Top layer 20, overlying the upper GaN channel layer 16 and optional AlN barrier 18, is an Al_(x)In_(y)Ga_(z)N cap layer, formed for example of AlGaN or alternatively of GaN, on the upper surface of which can be disposed conventional source, gate and drain elements (not shown in FIG. 1). The barrier layer 18 and cap layer 20 can be widely varied in composition and conformation, as well as in processing (e.g., doping, recessing, passivation, etc.). In the Al_(x)In_(y)Ga_(z)N cap layer, each of x, y and z has a value of from 0 to 1 inclusive, with x+y+z=1, and each of x, y and z can optionally vary with depth, so that an AlN/AlGaN/GaN cap or a graded AlInGaN layer may be present, in specific embodiments.

The (Al, In, Ga)N subchannel layer 14 in FIG. 1 is desirably as close to a monomolecular layer as possible, e.g., 1, 2 or 3 molecular layers in thickness, and most preferably is of monolayer thickness across the full area extent of the top surface of the lower GaN channel layer 12. The (Al, In, Ga)N subchannel layer may for example be formed of AlN and have a thickness on the order of 2.5 to 5 Angstroms, and the upper GaN channel layer 16 may have a channel thickness on the order of 30-50 Angstroms. The (Al, In, Ga)N subchannel layer can be formed by any suitable growth methodology.

As discussed herein above, it is desirable to keep the (Al, In, Ga)N subchannel layer as thin as possible, in order to maintain suitable electron density in the lower GaN channel layer and to minimize the negative spike in electron density in the vicinity of the AlN subchannel layer. It may also be beneficial to have a very low, e.g., monolayer, thickness in the subchannel, to achieve reduced alloy and roughness scattering, as well as reproducibility of the subchannel dimensions by deposition techniques such as atomic layer epitaxy (ALE).

The structure shown in FIG. 1 may be varied in relative thicknesses of component layers as may be necessary or desired in a specific application to achieve desired electron density and output performance. For example, by making the overlying GaN channel layer 16 thinner, the negative spike in electron density (associated with the subchannel layer) is rendered less severe, and electron density in the underlying GaN channel layer increases. One of skill in the art can readily determine the appropriate relative thicknesses of the component layers of the HEMT device as necessary or desirable in a specific device application, by empirical structures of the present invention.

FIG. 2 is a band diagram of the device of FIG. 1, showing that the AlN subchannel layer gives a step in the energy band and some spill-down of charge, with the upper GaN channel layer of higher electron content in relation to the lower GaN channel layer (GaN channel #2).

FIG. 3 is a graph of conduction band edge (curve A), E_(c), in electron volts (eV), and carrier concentration (curve B), in cm⁻³, as a function of depth, in Angstroms, for a structure including a 3 nm thick GaN channel and a 0.2 nm AlN undoped subchannel.

The FIG. 3 profile shows the upper GaN channel layer electron density having a roughly parabolic shape with a peak of about 5E19 cm⁻³ at a depth of about 270 Angstroms, and the lower GaN channel layer electron density exhibits a peak of about 2E18 cm⁻³ at a depth of about 310 Angstroms, with the AlN subchannel layer being centered at a depth of about 290 Angstroms in the structure.

FIG. 4 is a graph of conduction band edge (curve A), E_(c), in electron volts (eV), and carrier concentration (curve B), in cm⁻³, as a function of depth, in Angstroms, for a structure including a 3 nm thick GaN channel and a 0.3 nm AlN undoped subchannel. The profile shapes for the upper and lower GaN channel layers in FIG. 4 as compared to FIG. 3 shows that an increase in the subchannel thickness by 50% (0.3 nm vs. 0.2 nm) effects a more uniform distribution of charge between the respective channel layers, with the upper GaN layer nonetheless retaining more charge than the lower GaN channel layer.

FIG. 5 is a graph of conduction band edge (curve A), E_(c), in electron volts (eV), and carrier concentration (curve B), in cm⁻³, as a function of depth, in Angstroms, for a structure including a 4 nm thick GaN channel and a 0.2 nm AlN undoped subchannel.

In relation to the conduction band graphs of FIGS. 3 and 4, FIG. 5 shows the effect of increased thickness of the GaN channel layer. In the FIG. 5 structure, the upper GaN channel layer has 33.3% greater thickness (i.e., a 4 nm thick GaN channel layer) than the structures of FIGS. 3 and 4. Such increase in upper channel thickness increases the charge of the upper channel layer in relation to the charge of the lower channel layer.

including a 4 nm thick GaN channel and a 0.3 nm AlN undoped subchannel.

Comparing FIGS. 5 and 6, it is seen that increasing the subchannel AlN layer thickness increases the amount of charge in the lower channel GaN layer.

FIG. 7 is a graph of conduction band edge (curve A), E_(c), in electron volts (eV), and carrier concentration (curve B), in cm⁻³, as a function of depth, in Angstroms, for a structure including a 4 nm thick GaN channel and a 0.3 nm AlN doped with silicon at a doping density of 10¹³ atoms/cm².

The effect of silicon doping of the subchannel layer is shown in FIG. 7 as altering the relative charge of the respective upper and lower GaN channel layers, so that they are more nearly equal to one another, but with the upper GaN channel layer containing slightly more charge than the lower GaN channel layer. Total charge also is increased relative to an undoped structure.

FIG. 8 is a graph of conduction band edge (curve A), E_(c), in electron volts (eV), and carrier concentration (curve B), in cm⁻³, as a function of depth, in Angstroms, for a device structure including a 5 nm thick AlGaN channel, containing 5% aluminum in the AlGaN channel material.

FIG. 9 is a graph of conduction band edge (curve A), E_(c), in electron volts (eV), and carrier concentration (curve B), in cm⁻³, as a function of depth in Angstroms, for a device structure including a 2 nm GaN channel, a 0.3 nm undoped AlN layer, a 3 nm GaN channel and a 0.3 nm undoped AlN layer.

The features and advantages of the invention are more fully shown with respect to the following non-limiting examples.

Examples

Referring now to the further drawings FIGS. 10-12, FIG. 10 is a schematic representation of a HEMT device structure including an AlN barrier layer and characterized by a sheet mobility of ˜330 Ω/square, FIG. 11 is a schematic representation of a HEMT device structure including an AlGaN channel and an AlN barrier layer and characterized by a sheet mobility of ˜4601/square.

In each of FIGS. 10-12, the thicknesses of the respective layers in the device structure are set out in appropriate dimensional units of microns (μm) or nanometers (nm).

Each of the AlN barrier HEMT structures in FIGS. 10-12 was grown under substantially the same growth conditions as the others. All epitaxial III-Nitride layers were deposited by low pressure MOCVD (metalorganic chemical vapor deposition). Precursors used were trimethylgallium (TMGa), trimethylaluminum (TMAl), and ammonia (NH₃). The carrier gas was a mixture of hydrogen and nitrogen. The growth temperature was approximately 1000° C.

FIG. 10 schematically depicts an AlN barrier HEMT. This device exhibited enhanced mobility and reduced sheet resistivity of about 330 Ω/square attributable to the thin AlN barrier. The substrate was a 350 μm thick high-purity semi-insulating (HPSI) 4H—SiC substrate, on which was deposited an AlN nucleation layer at a thickness of 200 nm. Overlying the nucleation layer is a 1 μm thick GaN:Fe film, on which in turn was deposited a 1 μm thick layer of gallium nitride. On such GaN layer was deposited a 0.4 nm thick AlN barrier layer, which in turn was capped with a 25 nm thick layer of Al_(0.26)Ga_(0.74)N. This AlN barrier HEMT had a sheet resistivity of approximately 330 Ω/square.

FIG. 11 is a schematic representation of an AlGaN channel AlN barrier HEMT device, which had a same layer sequence as the HEMT device structure in FIG. 10, except that an additional layer was present in the FIG. 11 structure, between the 1 μm thick GaN layer and the 0.4 nm AlN barrier layer. This additional layer was a 6 nm Al_(0.06)Ga_(0.94)N channel layer. This AlGaN channel AlN barrier HEMT had a sheet resistivity of approximately 610 Ω/square. In relation to the FIG. 10 HEMT, the electron mobility in the FIG. 11 device was significantly reduced, and the sheet resistivity was increased by about 85%, an increase consistent with higher alloy scattering of electrons in the ternary channel.

FIG. 12 is a schematic representation of an AlN subchannel AlN barrier HEMT. This device structure had the same layer sequence as the HEMT device structure shown in FIG. 10, except that two additional layers were present in the FIG. 12 structure, between the 1 μm thick GaN layer and the 0.4 nm AlN barrier layer. These additional layers were a 0.3 nm thick

In relation to the HEMT device structure of FIG. 11, the HEMT device structure of FIG. 12 replaced the AlGaN channel of the FIG. 11 device with a GaN channel layer and an AlN subchannel layer. The HEMT device of FIG. 12 exhibited a sheet resistivity of approximately 460 Ω/square, still greater than the AlN barrier HEMT of FIG. 10, but significantly better (approximately 25% lower) than the AlGaN channel structure HEMT of FIG. 11.

INDUSTRIAL APPLICABILITY

The present invention provides a HEMT device structure that enables control of electron distribution to produce improved device linearity, without substantial adverse affect on electron mobility characteristics of the device, with a GaN channel and (Al, In, Ga)N subchannel arrangement that effectively disperses the 2DEG throughout the channel of the device, thereby rendering the device more linear in character (relative to a corresponding device lacking the (Al, In, Ga)N subchannel layer) without substantial loss of electron mobility. The device structure of the invention has application in wireless communications, low noise amplifiers, V-band power amplifiers, and millimeter-wave signal processing. 

1. Electronic component comprising an emitter comprising a metal complex containing 2-(3-thienyl)-pyridine ligands wherein the metal complex is of general formula 1 or 2:

wherein M is a heavy metal, X, Y and LL are ligands, which independently of one another are charged or uncharged and from which essentially no emission comes, R¹ and R² independently of one another may be present one or more times on the respective cycle and are independently selected from F, Cl, Br, I, NO₂, CN, a straight-chain or branched or cyclic alkyl or alkoxy group with 1 to 20 carbon atoms, wherein one or more non-adjacent CH₂ groups may be replaced by —O—, —SiR³ ₂—, —S—, —NR³— or —CONR³— and wherein one or more H atoms may be replaced by F, or an aryl or heteroaryl group with 4 to 14 C atoms, which may be substituted with one or more non-aromatic radicals R¹ or R²; wherein a number of substituents R¹ and/or R², both on the same ring and on the two different rings, may together form a further monocyclic or polycyclic ring system; R³ is identical or different each time it occurs and is selected from H or an aliphatic or aromatic hydrocarbon radical with 1 to 20 carbon atoms; n=1-3, m and l independently of one another are 0-4 where 2n+m+l=4 or 6, or p=0-2 where 2n+2p=4 or
 6. 2. Electronic component according to claim 1, characterized in that the heavy metal is selected from Pt(II), Pt(IV), Re(I), Os(II), Ru(II), Ir(I), Ir(III), Au(I), Au(III), Hg(I), Hg(II) and Cu(I).
 3. Electronic component according to claim 1, characterized in that X and Y independently of one another are ligands with a single negative charge or neutral monodentate ligands.
 4. Electronic component according to claim 3, characterized in that X and Y independently of one another are selected from F⁻, Cl⁻, Br⁻, I⁻, CN⁻, NCO⁻, SCN⁻, R⁴S⁻, R⁴O⁻, R⁴C═C⁻, R⁴COO⁻, NO₃ ⁻, amine, phosphane, arsane, nitrile, isonitrile, CO, carbene, ethers and thio-ethers, wherein R⁴ is an organic radical with 1 to 15 carbon atoms, preferably alkyl.
 5. Electronic component according to claim 1, characterized in that LL, preferably with a single negative charge, is a chelating ligand and/or a cyclometalating ligand.
 6. According to claim 5, characterized in that LL is selected from β-diketonate, β-diketoiminate, [(pyrazolyl)₂H]⁻, [(pyrazolyl)₂BR⁵ ₂]⁻, [pyrazolyl₃BH]⁻, [pyrazolyl₄B]⁻, (triazolyl)₂BH₂ ⁻, (triazolyl)₃BH⁻, (triazolyl)₄B⁻, (Ph₂PCH₂)₂BR⁵ ₂ ⁻, R⁵COO⁻, NO₃ ⁻, diamine, diphosphane, diarsane, dinitrile, diisonitrile, dialkyl ethers and dialkyl (thio)ethers, wherein R⁵ is an organic radical with 1 to 15 carbon atoms, preferably alkyl.
 7. Electronic component according to claim 1, characterized in that the metal complex is used as a triplet emitter.
 8. (canceled)
 9. Electronic component according to claim 1, in the form of an organic light-emitting diode (OLED).
 10. Electronic component according to claim 9, characterized in that the organic light-emitting diode contains the complex in a concentration of 2-20 percent by weight, preferably 5-8 percent by weight, preferably in an electron transport layer. 